AstraZeneca gets EU COVID-19 third dose booster nod

AstraZeneca's COVID-19 vaccine has been granted approval in the European Union (EU) by the European Medicine Agency (EMA) as a third dose booster in adults.

Healthcare professionals can now use AstraZeneca COVID-19 vaccine as a third dose booster in patients previously given a primary vaccine schedule of either AstraZeneca COVID-19 vaccine or an EU-approved mRNA COVID-19 vaccine.

The authorisation is based on a review by the Committee for Medicinal Products for Human Use (CHMP) of the substantial body of evidence demonstrating an increased immune response after a third dose booster with AstraZeneca COVID-19 vaccine following a primary vaccine schedule of either AstraZeneca COVID-19 vaccine or an mRNA COVID-19 vaccine.

Although more than 65% of the global population has received at least one dose of a COVID-19 vaccine, there remains a significant challenge to ensure people receive both their primary vaccine schedule and third dose booster and healthcare professionals now have greater flexibility in their choice of vaccine.

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“The marketing authorisation for AstraZeneca’s COVID-19 vaccine as a third dose booster is an important step towards our goal of providing continued protection against COVID-19 for all populations. Ensuring a longer duration of immune protection is essential to the long-term management of COVID-19 globally and boosters can address the waning of protection over time that has been seen with all primary vaccine schedules to date,” Mene Pangalos, Executive Vice President, BioPharmaceuticals R&D, AstraZeneca, reacted.

There’s a substantial body of evidence supporting AstraZeneca COVID-19 vaccine as a third dose booster following all primary vaccination schedules tested to date including AstraZeneca COVID-19 vaccine, mRNA vaccines and CoronaVac.

AstraZeneca COVID-19 vaccine is already authorised as a homologous booster (patients previously given a primary vaccine schedule of AstraZeneca COVID-19 vaccine) in the UK and several countries in Asia and Latin America.

It’s also been authorised as a heterologous booster (patients previously given a primary vaccine schedule of either a viral vector vaccine other than AstraZeneca COVID-19 vaccine or an inactivated vaccine or an mRNA COVID-19 vaccine) in a number of non-EU countries.

And it’s estimated to have helped prevent 50 million COVID-19 cases, five million hospitalisations and saved more than one million lives based on model outcomes assessing COVID-19 worldwide.

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